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Congenital myopathy v3.89 SCN4A Arina Puzriakova Phenotypes for gene: SCN4A were changed from congenital myopathy to Congenital myopathy, MONDO:0019952
Congenital myopathy v1.120 SCN4A Rachael Mein edited their review of gene: SCN4A: Changed publications: 26700687; Changed phenotypes: congenital myopathy
Congenital myopathy v1.76 SCN4A Louise Daugherty reviewed gene: SCN4A: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Congenital myopathy v1.75 SCN4A Rachael Mein reviewed gene: SCN4A: Rating: GREEN; Mode of pathogenicity: ; Publications: 12207937; Phenotypes: nemaline myopathy, Nemaline Myopathy, Recessive, Nemaline myopathy 2, autosomal recessive, 256030; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Congenital myopathy v1.74 SCN4A Louise Daugherty Source NHS GMS was added to SCN4A.
Congenital myopathy v1.73 SCN4A Louise Daugherty Source London South GLH was added to SCN4A.
Rating Changed from Green List (high evidence) to Green List (high evidence)
Congenital myopathy SCN4A Helen Brittain marked SCN4A as ready
Congenital myopathy SCN4A Helen Brittain classified SCN4A as green
Congenital myopathy SCN4A Helen Brittain commented on SCN4A
Congenital myopathy SCN4A Anna Sarkozy reviewed SCN4A